Citation: JIAO Hua-Jing, WANG Qi, DING Liu-Liu, LU Chang-Sheng. Maleonitriledithiolate Modified β-Cyclodextrin: Self-Inclusion and Response to Metal Ions[J]. Chinese Journal of Inorganic Chemistry, ;2015, 31(7): 1269-1277. doi: 10.11862/CJIC.2015.180
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The self-inclusion of maleonitriledithiolate-modified β-Cyclodextrin (mono[6-deoxy-6-(2-butene-dinitrile-2,3-dimercapto)]-β-Cyclodextrin, 6-mnt-β-Cyclodextrin) was studied by circular dichroism (CD) spectroscopy, 1H NMR spectroscopy, isothermal titration calorimetry (ITC), and chemical titration methods. Chemical titration results indicate that sodium dodecyl sulfate (SDS) is able to effectively dissociate the configuration of 6-mnt-β-Cyclodextrin, as well as Cu2+ and Co2+ do in solution. The experimental data suggest that 6-mnt-β-Cyclodextrin prefers self-inclusion in aqueous solution, which could be reversibly unlocked by metal ions. In its unlocked conformation, 6-mnt-β-Cyclodextrin is able to include Neutral Red (NR) and exhibits host-guest interactions. Upon removal of the "key" metal ion, 6-mnt-β-Cyclodextrin liberates the guest molecule and restores its self-inclusion. Therefore, the maleonitriledithiolate-modified cyclodextrin host exhibits potential to controllably uptake and release its guest by selected metal ion coordination.
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